Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_assertion description "[Deficiency of the paternal 15q11-q13 snoRNA HBII-85 locus is necessary to cause the neurodevelopmental disorder Prader-Willi syndrome (PWS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_assertion evidence source_evidence_literature NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_assertion SIO_000772 19656775 NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_assertion wasDerivedFrom befree-2016 NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_assertion wasGeneratedBy ECO_0000203 NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.
- befree-2016 importedOn "2016-02-19" NP755572.RA3BPhczU7q12ZxfaLuRN2-YSDDcCCO7M37QjdKdTf52s130_provenance.